DFMO Maintenance for Patients With Relapsed/Refractory Ewing Sarcoma or Osteosarcoma

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

The purpose of this study is to determine the feasibility of administering DFMO to patients with relapsed Ewing sarcoma and osteosarcoma who have completed all planned therapy and have no evidence of disease.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 39
Healthy Volunteers: f
View:

• Patients \< 40 years of age at the time of enrollment

• Diagnosis of relapsed osteosarcoma or relapsed Ewing sarcoma who have completed all planned therapy for their relapse, as described in the protocol, and have no evidence of disease

• Patients must have a performance status corresponding to Eastern Cooperative Oncology Group (ECOG) scores of 0, 1, or 2

• Adequate bone marrow function defined as:

• Peripheral absolute neutrophil count (ANC) greater or equal to 750/microliters

• Platelet count greater or equal to 75,000/microliters (transfusion independent)

• Adequate renal function defined by serum creatinine based on age and gender

• Adequate liver function defined as:

• Total bilirubin ≤ 1.5 x the upper limit of normal (ULN) for age AND

• SGPT (ALT) ≤ 5.0 x ULN for age. For this study the ULN is 45 U/L

Locations
United States
New York
Montefiore Medical Center
RECRUITING
The Bronx
Contact Information
Primary
Rebecca Zylber, MSN
rzylber@montefiore.org
718-741-2356
Backup
Lara Fabish, MSN
lfabish@montefiore.org
718-741-2356
Time Frame
Start Date: 2025-04-07
Estimated Completion Date: 2030-04
Participants
Target number of participants: 15
Treatments
Experimental: Treatment with DFMO
DFMO will be administered orally every 12 hours in 28-day cycles at the FDA approved dosages based on the patient's body surface area (BSA). DFMO tablets are 192 mg.~* Patients with a BSA \< 1.5 m2 will take 768 mg (four tablets) orally twice a day.~* Patients with a BSA 0.75 to 1.5 m2 will take 576 mg (three tablets) orally twice a day.~* Patients with a BSA of 0.5 to \< 0.75 m2 will take 384 mg (two tablets) orally twice a day.~* Patients with a BSA of 0.25 to \< 0.5 m2 will take 192 mg (one tablet) orally twice a day.
Sponsors
Leads: Montefiore Medical Center
Collaborators: Johns Hopkins University

This content was sourced from clinicaltrials.gov

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